EP0236940A2

EP0236940A2 - Alpha-heterocycle substituted tolunitriles

Info

Publication number: EP0236940A2
Application number: EP87103099A
Authority: EP
Inventors: Robert Mathews Bowman; Ronald Edward Steele; Leslie Johnston Browne
Original assignee: Ciba Geigy AG
Current assignee: Novartis AG
Priority date: 1986-03-07
Filing date: 1987-03-05
Publication date: 1987-09-16
Anticipated expiration: 2007-03-05
Also published as: MA20888A1; SU1577695A3; IL81746A0; TNSN87033A1; DK117687D0; CZ279028B6; KR910000482B1; DE3787480T2; EP0236940A3; PL151490B1; CS8701512A2; DE19775016I2; PL264460A1; JPH0755930B2; BG45701A3; SK279103B6; SK736787A3; NO870937L; SK279102B6; US4749713A

Abstract

Compounds of the formula I

wherein the groups R, R₀, R₁, R₂ and W are as defined in the specification, exhibit valuable pharmacological properties, especially as aromatase inhibitors.

Description

The invention relates to certain heterocycle-substituted tolunitriles.
Particularly the invention relates to the use of compounds of the formula I
wherein R and R_a independently represent hydrogen or lower alkyl; or R and R_o located on adjacent carbon atoms and together when combined with the benzene ring to which they are attached form a naphthalene or tetrahydro-naphthalene ring; R, and R₂ independently represent hydrogen, lower alkyl, (lower alkyl, aryl or aryl-lower alkyl)-thio, lower alkenyl, aryl, aryl-lower alkyl, C₃-C₆-cycloalkyl, or C₃-C₆-cycloalkyl-lower alkyl; or R, and R_z combined represent lower alkylidene, mono-or di-aryl-lower alkylidene; R, and R₂ combined also represent C₄-C₆-straight chain alkylene, lower alkyl-substituted straight chain alkylene or ortho-phenylene bridged-C₂-C₄-straight chain alkylene, each forming with the carbon atom attached thereto a corresponding optionally substituted or benzo-fused 5-, 6-or 7-membered ring; W represents 1-imidazolyl, 1-(1,2,4 or 1,3,4)-triazolyl or 3-pyridyl; or W represents 1-imidazolyl, 1-(1,2.4 or 1.3,4)-triazolyl or 3-pyridyl substituted by lower alkyl; and pharmaceutically acceptable salts thereof; as pharmaceutical agents or for the manufacture of pharmaceutical preparations, to new compounds of this kind, a process for the manufacture of the latter and pharmaceutical compositions comprising the latter.
The compounds of the invention which possess an asymmetric carbon atom exist as racemates and the R and S enantiomers thereof. The present invention is intended to include these forms, also diastereoisomers and mixtures thereof if two or more asymmetric centers are present, as well as geometric isomers, e.g. cis and trans isomers, if a double bond is present in the molecule.
The general definitions used herein, unless denoted otherwise, have the following meanings within the scope of the present invention.
The term "lower" referred to above and hereinafter in connection with organic radicals or compounds respectively preferably defines such with up to and including 7, preferably up to and including 4 and advantageously one or two carbon atoms.
A lower alkyl group preferably contains 1-4 carbon atoms and represents for example ethyl, propyl, butyl or advantageously methyl.
A lower alkenyl group preferably contains 2-4 carbon atoms and represents for example allyl or crotyl.
A lower alkoxy group preferably contains 1-4 carbon atoms and represents for example methoxy, propoxy, isopropoxy or advantageously ethoxy.
Halogen preferably represents chlorine, but may also be bromine, fluorine or iodine.
Acyl in acyloxy represents lower alkanoyl, aroyl, lower alkoxycarbonyl, or N,N-di-lower alkylcarbamoyl, preferably lower alkanoyl.
Lower alkanoyl is preferably acetyl, propionyl, butyryl, or pivaloyl, especially acetyl.
Aroyl is preferably benzoyl; and also e.g. benzoyl substituted by one or two of lower alkyl, lower alkoxy, halogen or trifluoromethyl; aroyl is also e.g. thienoyl, pyrroloyl, 2-, 3-or 4-pyridylcarbonyl, advantageously nicotinoyl.
Lower alkanoyloxy is preferably acetoxy; and also e.g. pivaloyloxy or propionyloxy.
Aroyloxy is preferably benzoyloxy; and also e.g. benzoyloxy substituted on the benzene ring by one or two of lower alkyl, lower alkoxy, halogen or trifluoromethyl.
Heteroaroyloxy is preferably 2-, 3-or 4-pyridylcarbonyloxy, advantageously nicotinoyloxy.
Aryl represents a carbocyclic or heterocyclic aromatic radical comprising e.g. optionally substituted phenyl, naphthyl, pyridyl, thienyl, indolyl or furyl, preferably phenyl, naphthyl, pyridyl, thienyl, indolyl or furyl, and especially phenyl.
A carbocyclic aromatic radical represents preferably phenyl or phenyl substituted by one or two substituents selected from lower alkyl, lower alkoxy, hydroxy, acyloxy, nitro, amino, halogen, trifluoromethyl, cyano, carboxy, carboxy functionalized in form of a pharmceutically acceptable ester or amide, lower alkanoyl, aroyl, lower alkylsulfonyl, sulfamoyl, N-lower alkylsulfamoyl and N,N-di-lower alkylsulfamoyl; also 1-or 2-naphthyl, optionally substituted by lower alkyl, lower alkoxy, cyano or halogen.
A heterocyclic aromatic radical represents particularly thienyl, indolyl, pyridyl, furyl; and also e.g. a said heterocyclic radical monosubstituted by lower alkyl, lower alkoxy, cyano or halogen.
Thienyl represents 2-or 3-thienyl, preferably 2-thienyl.
Pyridyl represents 2-, 3-or 4-pyridyl, preferably 3-or 4-pyridyl advantageously 3-pyridyl.
Furyl represents 2-or 3-furyl, preferably 3-furyl.
Indolyl represents preferabaly 3-indolyl.
Carboxy functionalized in form of a pharmaceutically acceptable ester represents preferably lower alkoxycarbonyl; and also e.g. aryl-lower alkoxycarbonyl, e.g. benzyloxycarbonyl or pyridylmethoxycarbonyl; lower alkanoyloxy-substituted lower alkoxycarbonyl, e.g. pivaloyloxymethoxycarbonyl; or 3-phthalidoxycarbonyl.
Carboxy functionalized in form of a pharmaceutically acceptable amide represents preferably carbamoyl, N-mono-lower alkylcarbamoyl or N,N-di-lower alkylcarbamoyl.
Aryl-lower alkyl represents preferably arylmethyl or arylethyl in which aryl represents a carbocyclic or heterocyclic aromatic radical as defined above, advantageously optionally substituted phenyl as defined above.
Lower alkylidene represents preferably straight chain lower alkylidene, advantageously methylidene or ethylidene.
C₄-C₆-alkylene represents advantageously butylene or pentylene.
Ortho-phenylene bridged-C₂-C.-straight chain alkylene represents preferably ortho-phenylene bridged CH₂CH₂.
C₃-C₆-cycloalkyl represents preferably cyclopentyl or cyclohexyl.
Pharmaceutically acceptable salts represent acid addition salts with conventional acids, for example mineral acids, e.g. hydrochloric acid, sulfuric or phosphoric acid, or organic acids, for example aliphatic or aromatic carboxylic or sulfonic acids, e.g. acetic, propionic, succinic, glycolic, lactic, malic, tartaric, citric, ascorbic, maleic, fumaric, hydroxymaleic, pyruvic, phenylacetic, benzoic, 4-aminobenzoic, anthranilic, 4-hydroxybenzoic, salicylic, 4-aminosalicylic, pamoic, gluconic, nicotinic, methanesulfonic, ethanesulfonic, halobenzenesulfonic, toluenesulfonic, naphthalenesulfonic, sulfanilic or cyclohexylsulfamic acid; also amino acids, such as arginine and lysine. For compounds of the invention having acidic groups, for example a free carboxy group, pharmaceutically acceptable salts also represent metal or ammonium salts, such as alkali metal or alkaline earth metal salts, e.g. sodium, potassium, magnesium or calcium salts, as well as ammonium salts, which are formed with ammonia or suitable organic amines.
The compounds of the instant invention have valuable pharmacological properties. For example, they are useful as inhibitors of aromatase activity and inhibitors or estrogen biosynthesis in mammals, and for treating conditions responsive thereto. These compounds inhibit the metabolic conversion of androgens to estrogens in mammals. Thus, the compounds of the invention are useful e.g. in the treatment of gynecomastia, i.e. male breast development, by inhibiting the aromatization of steroids in males susceptible to this condition. Moreover, the compounds of the invention are useful e.g. in the treatment of estrogen dependent diseases in females, for example estrogen dependent female breast cancer, especially in postmenopausal females, by inhibiting estrogen biosynthesis.
These effects are demonstrable in in vitro assay tests or in vivo animal tests using advantageously mammals, e.g. guinea pigs, mice, rats, cats, dogs, or monkeys. The applied dosage may range between about 0.001 and 30 mg/kg, preferably between about 0.001 to 5 mg/kg.
The in vitro inhibition of aromatase activity of the compounds of the present invention can be demonstrated e.g. as follows: A microsomal fraction is prepared from human placenta by the method essentially as described by Thompson and Siiteri, J. Biol. Chem. 249, 5364 (1974). The microsomal preparation so obtained is lyophilized and stored at -40°C. The assay is conducted substantially as described by Thompson and Siiteri. IC_so values can be determined graphically as the concentration of test compound at which the aromatization of androstenedione to estrone is reduced to 50% of control value. The compounds of the invention are effective at concentrations of about 1 0-'M or above.
The in vivo inhibition of aromatase activity of the compounds of the present invention can be demonstrated e.g. by measuring the inhibition of estrogen synthesis in rats. The inhibition of estrogen synthesis, indicative of aromatase inhibition, is calculated from the ovarian estrogen content in treated as compared to control animals. The compounds of the invention inhibit estrogen synthesis at a dose of about 3 ug/kg p.o. or above in the female rat.
The in vivo inhibition of aromatase activity can be also assessed e.g. as follows: Androstenedione (30 mg/kg subcutaneously) alone and together with the aromatase inhibitor under investigation (orally or subcutaneously) is administered to immature female rats once daily for 4 days. After the fourth application, the rats are sacrificed and their uteri removed and weighed. The inhibition of aromatase can be assessed by determining the extent to which the uterine hypertrophy elicited by androstenedione alone is suppressed by coadministration of the aromatase inhibitor.
The antitumor activity, especially in estrogen-dependent tumors, can be demonstrated in vivo e.g. in dimethylbenzanthracene (DMBA)-induced mammary tumors in female Sprague-Dawley rats [see Proc. Soc. Exp. Biol. Med. 160, 296-301 (1979)]. Compounds of the invention cause regression of existing tumors and suppress the appearance of new tumors at daily doses of about 0.1 mg/kg p.o. or above.
Furthermore, the compounds of the invention are essentially devoid of cholesterol side chain cleavage inhibitory activity and do not induce adrenal hypertrophy at effective aromatase inhibitory doses.
Due to their pharmacological properties as selective aromatase inhibitors, the compounds of the invention are useful for the inhibition of estrogen biosynthesis in mammals and the treatment of estrogen dependent disorders responsive thereto, such as mammary tumors (breast carcinoma), endometriosis, premature labor and endometrial tumors in females, as well as gynecomastia in males.
Preferred is the use of the compounds of formula I wherein R and R_o represent independently hydrogen or lower alkyl; or R and R_o located on adjacent carbon atoms and together when combined with the benzene ring to which they are attached form a naphthalene or tetrahydronaphthalene ring; R, represents hydrogen, lower alkyl, aryl, aryl-lower alkyl or lower alkenyl; R₂ represents hydrogen, lower alkyl, aryl, aryl-lower alkyl, (lower alkyl, aryl or aryl-lower alkyl)-thio or lower alkenyl; or R, and R₂ combined represent lower alkylidene or C₄-C₆ alkylene; W has meaning given above; and aryl within the above definitions represents phenyl or phenyl substituted by one or two substituents selected from lower alkyl, lower alkoxy, hydroxy, acyloxy, nitro, amino, halogen, trifluoromethyl, cyano, carboxy, carboxy functionalized in form of a pharmaceutically acceptable ester or amide, lower alkanoyl, aroyl, lower alkylsulfonyl, sulfamoyl, N-lower-alkylsulfamoyl or N,N-di-lower alkylsulfamoyl; or aryl within the above definitions also represents a heterocyclic aromatic radical selected from thienyl, indolyl, pyridyl and furyl, or a said heterocyclic radical monosubstituted by lower alkyl, lower alkoxy, cyano or halogen; and pharmaceutically acceptable salts thereof.
Particularly preferred is the use of said compounds of formula I wherein R, represents hydrogen; and W, R, R_o, R₂ as well as R, and R2 combined have meaning as defined above.
Furthermore, the invention relates to the compounds of the formula I
wherein R and R_o independently represent hydrogen or lower alkyl; or R and R_o located on adjacent carbon atoms and together when combined with the benzene ring to which they are attached form a naphthalene or tetrahydro-naphthafene ring; R, represents hydrogen; R₂ represents hydrogen, lower alkyl, lower alkenyl, aryl, aryl-lower alkyl, C₃-C₆-cycloalkyl, or C₃-C₆cycloalkyl-lower alkyl; or R, and R₂ combined represent lower alkylidene, or mono-or di-aryl-lower alkylidene; R, and R₂ combined also represent C₄-C₆-straight chain alkylene, lower alkyl-substituted straight chain alkylene or ortho-phenylene bridged-C₂-C₄-straight chain alkylene, to form with the carbon atom attached thereto a corresponding optionally substituted or benzo-fused 5-, 6-or 7-membered ring; W represents 1-imidazolyt, 1-(1,2,4 or 1,3,4)-triazolyl or 3-pyridyl; or W represents 1-imidazolyl, 1-(1,2,4 or 1,3,4)-triazolyl or 3-pyridyl substituted by lower alkyl; and pharmaceutically acceptable salts thereof.
Especially preferred are the compounds of the formula 1, wherein R and R_o represent hydrogen; or R and R_o located on adjacent carbon atoms and together when combined with the benzene ring to which they are attached form a naphthalene ring; R, represents hydrogen; R₂ represents hydrogen, lower alkyl, aryl or aryl-lower alkyl; or R, and R₂ combined represent lower alkylidene or di-aryl-lower alkylidene; R, and R₂ combined also represent C₄-C₆-straight chain alkylene or ortho-phenylene bridged-C_zCa-straight chain alkylene, to form with the carbon atom attached thereto a corresponding optionally benzo-fused 5-, 6-or 7- membered ring; W represents 1-imidazolyl, 1-(1,2,4 or 1,3,4)-triazolyl, 3-pyridyl, or 1-imidazolyl substituted by lower alkyl; and aryl within the above definitions represents phenyl or phenyl substituted by lower alkyl, lower alkoxy, hydroxy, halogen, trifluoromethyl or cyano; thienyl or pyridyl; and pharmaceutically acceptable salts thereof.
Also preferred are the compounds of formula I, wherein R and R_o independently represent hydrogen or lower alkyl; or R and R_o located on adjacent carbon atoms and together when combined with the benzene ring to which they are attached form a naphthalene or tetrahydro-naphthalene ring; R, represents hydrogen; R₂ represents hydrogen, lower alkyl, lower alkenyl, aryl, or aryl-lower alkyl; or R, and R₂ combined represent lower alkylidene or C₄-C₆-alkylene; W represents 1-imidazolyl or 1-imidazolyl substituted by lower alkyl; and aryl within the above definitions represents phenyl or phenyl substituted by one or two substituents selected from lower alkyl, lower alkoxy, hydroxy, acyloxy, nitro, amino, halogen, trifluoromethyl, cyano, carboxy, carboxy functionalized in form of a pharmaceutically acceptable ester or amide, lower alkanoyl, aroyl, lower alkylsulfonyl, sulfamoyl, N-lower alkylsulfamoyl or N,N-di-lower alkylsulfamoyl; or aryl within the above definitions also represents a heterocyclic aromatic radical selected from thienyl, indolyl, pyridyl and furyl, or a said heterocyclic radical monosubstituted by lower alkyl, lower alkoxy, cyano or halogen; and pharmaceutically acceptable salts thereof.
Further preferred are the compounds of formula II
wherein R₁ represents hydrogen; R₂' represents hydrogen, lower alkyl, phenyl, pyridyl, thienyl or benzyl; or R₂' represents phenyl or benzyl, each monosubstituted on the phenyl ring by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, aroyloxy, nitro, halogen, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; or R,' and R₂' combined represent together lower alkylidene, benzylidene or diphenylmethylidene; or R,' and R₂' combined represent together C₄-C₆ straight chain alkylene; R, represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.
Particularly preferred are the compounds of formula II wherein R,' represents hydrogen; R₂' represents hydrogen, lower alkyl, pyridyl, benzyl or phenyl; or R; represents benzyl or phenyl, each monosubstituted on phenyl by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, halogen, nitro, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; R₃ represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.
Preferred in turn are the compounds of formula II wherein R,' represents hydrogen; R2 represents hydrogen, lower alkyl, benzyl, phenyl, or 3-or 4-pyridyl; or R; represents phenyl or benzyl, each monosubstituted on phenyl by cyano, halogen, lower alkoxy, lower alkyl or trifluoromethyl; R₃ represents hydrogen or lower alkyl at the 4-or 5-position; and pharmaceutically acceptable salts thereof.
Particularly preferred are the compounds of formula II wherein R; represents unsubstituted or monosubstituted phenyl or benzyl, or pyridyl, as defined hereinabove.
Most preferred are the compounds of formula III
wherein R₂' represents 3-pyridyl, p-cyanobenzyl or p-cyanophenyl; and pharmaceutically acceptable salts thereof.
A particular embodiment of the invention relates to the compounds of formula I wherein R and R_o are located on adjacent carbon atoms and together when combined with the benzene ring to which they are attached form a naphthalene or tetrahydro-naphthalene ring.
A preferred embodiment thereof relates to the naphthonitriles of formula IV
wherein R,' represents hydrogen; R₂' represents hydrogen, lower alkyl, phenyl, lower alkylthio, phenyl-lower alkylthio, phenylthio, pyridyl, thienyl or benzyl; or R₂' represents phenyl, phenyl-lower alkylthio, phenylthio or benzyl, each monosubstituted on the phenyl ring by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, aroyloxy, nitro, halogen, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; or R,' and R₂' combined represent together lower alkylidene, benzylidene, diphenylmethylidene; or R,' and R₂' combined represent together C₄-C₆ straight chain alkylene; R₃ represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.
Particularly preferred are the compounds of formula IV wherein R₁' represents hydrogen; R₂' represents hydrogen, lower alkyl, pyridyl; or R; represents benzyl or phenyl, each unsubstituted or monosubstituted on phenyl by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, halogen, nitro, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; R₃ represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.
Preferred in turn are the compounds of formula IV wherein R₁' represents hydrogen; R₂' represents hydrogen, lower alkyl, benzyl, phenyl, or 3-or 4-pyridyl; or R₂` represents phenyl or benzyl, each monosubstituted on phenyl by cyano, halogen, lower alkoxy, lower alkyl or trifluoromethyl; R₃ represents hyrogen or lower alkyl at the 4-or 5-position; and pharmaceutically acceptable salts thereof.
Most preferred are the compounds of formula IV wherein R₁' and R, represent hydrogen; R₂' represents 3-pyridyl, p-cyanobenzyl or p-cyanophenyl; and pharmaceutically acceptable salts thereof.
Another specific preferred embodiment of the invention relates to compounds of formula I wherein W represents 1-(1,2,4)-triazolyl or 1-(1,2,4)-triazolyl substituted by lower alkyl. Preferred thereof are the compounds of formula V
wherein R₁' represents hydrogen; R₂' represents hydrogen, lower alkyl, phenyl, pyridyl, thienyl or benzyl; or R₂' represents phenyl or benzyl, each monosubstituted on the phenyl ring by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, aroyloxy, nitro, halogen, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; or R,' and R₂' combined represent together lower alkylidene, benzylidene or diphenylmethylidene; or R,' and R₂' combined represent together C₄-C₆ straight chain alkylene; R₃' represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.
Particularly preferred are the compounds of formula V wherein R,' represents hydrogen; R; represents hydrogen, lower alkyl or pyridyf; or R₂' represents benzyl or phenyl, each unsubstituted or monosubstituted on phenyl by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, halogen, nitro, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; R₃' represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.
Preferred in turn are the compounds of formula V wherein R,' represents hydrogen; R; represents hydrogen, lower alkyl, benzyl, phenyl, or 3-or 4-pyridyl; or R; represents phenyl or benzyl, each monosubstituted on phenyl by cyano, halogen, lower alkoxy, lower alkyl or trifluoromethyl; R₃' represents hydrogen or lower alkyl; and pharmaceutically accpetable salts thereof.
Most preferred are the compounds of formula V wherein R₁' and R₃' represent hydrogen; R₂' represents 3-pyridyl, p-cyanobenzyl or p-cyanophenyl; and pharmaceutically acceptable salts thereof.
A further specific embodiment of the invention relates to compounds of the formula I wherein W represents a 3-pyridyl group, particularly the compounds of formula VI
wherein R,' represents hydrogen; R₂' represents hydrogen, lower alkyl, phenyl, lower alkylthio, phenyl-lower alkylthio, phenylthio, pyridyl, thienyl, benzyl; or R₂` represents phenyl, phenyl-lower alkylthio, phenylthio or benzyl, each monosubstituted on the phenyl ring by cyano, lower alkyl, loewr alkoxy, hydroxy, lower alkanoyloxy, aroyloxy, nitro, halogen, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; or R,' and R₂' combined represent together lower alkylidene, benzylidene or diphenylmethylidene; or R₁' and R₂' combined represent together C₄-C₆ straight chain aJkylene; R, represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.
Particularly preferred are the compounds of formula VI wherein R,' represents hydrogen; R₂' represents hydrogen, lower alkyl, pyridyl; or R₂' represents benzyl or phenyl each unsubstituted or monosubstituted on phenyl by cyano, tower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, halogen, nitro, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; R, represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.
Preferred in turn are the compounds of formula VI wherein R,' and R3 represent hydrogen; R₂' represents hydrogen, lower alkyl, benzyl, phenyl, or 3-or 4-pyridyl; or R₂' represents phenyl or benzyl each substituted on phenyl by cyano, halogen, lower alkoxy, lower alkyl or trifluoromethyl; and pharmaceutically acceptable salts thereof.
Most preferred are the compounds of formula VI wherein R,' and R₃ represent hyrogen; R₂' represents 3-or 4-pyridyl, p-cyanobenzyl or p-cyanophenyl; and pharmaceutically acceptable salts thereof.
A specific embodiment of the invention relates to the compounds of formula I wherein W represents 1-imidazolyl or 1-imidazolyl substituted by lower alkyl; another embodiment relates to the compounds of formula I wherein W represents 1-(1,2,4 or 1,3,4)-triazolyl or 1-(1,2,4 or 1,3,4)-triazolyl substituted by lower alkyl; a further embodiment relates to the compounds of formula I wherein W represents 3-pyridyl or 3-pyridyl substituted by lower alkyl. Further particular embodiments relate to compounds of formula I wherein R and R_o represent hydrogen or lower alkyl; also those wherein R and R_o together with the benzene ring to which they are attached form a naphthalene or tetrahydro-naphthalene ring.
Preferred are the compounds of formula I wherein the
grouping is attached para to the cyano group. Above all are preferred the compounds of the invention described in the examples and pharmaceutically acceptable salts thereof.
The compounds of formula I or II-VI may be prepared e.g. as follows:

a) for compounds of formula I wherein W represents 1-imidazolyl or 1-triazolyl each optionally substituted by lower alkyl, condensing a compound of the formula VII W'-H (VII) wherein W' represents 1-imidazolyl or 1-triazolyl each optionally substituted by lower alkyl, or an N-protected derivative thereof, with a reactive esterified derivative of a compound of the formula VIII
wherein R, R_o, R, and R2 have meaning as defined herein for formula I;
b) for compounds wherein W represents 3-pyridyl optionally substituted by lower alkyl, dehalogenating a compound of the formula IX
wherein W" represents 3-pyridyl optionally substituted by lower alkyl, X represents halogen, preferably chloro, R and R_o have meaning as defined herein for compounds of formula I and R, has meaning as defined herein for formula I; and if required reacting the resulting product of formula X
with a reactive derivative of the radical R₂ using process c) below;
c) condensing under basic conditions a compound of the formula XI
(being a compound of formula I wherein R, and R₂ represent hydrogen) wherein R, R_o and W have meaning as defined herein for formula I, with a reactive functional derivative of a radical R, or R₂ (R, or R₂ not representing hydrogen), so as to obtain a compound of formula I wherein only one of R, and R2 represents hydrogen; or similarly condensing a compound of formula I so obtained with a reactive functional derivative of a radical R, or R2 (R, or R₂ not representing hydrogen) to obtain a compound of formula I wherein neither R, nor R2 represents hydrogen; or condensing a compound of the formula XI with a reactive bifunctional derivative of R, and R₂ combined representing C₄-C₆ straight alkylene, lower alkyl substituted C₄-C₆ straight chain alkylene or 1,2-phenylene-bridged-C₂-C₄ straight chain alkylene to obtain a corresponding compound of formula I;
d) converting R_s to cyano in a compound of the formula XII
wherein W, R, R_o, R, and R₂ have meaning as defined above and R₅ represents a group or radical that can be converted to the cyano group; and/or converting a compound of formula I into another compound of formula 1; and/or converting a free compound into a salt, and/or converting a salt into a free compound or into another salt; and/or separating a mixture of isomers or racemates into the single isomers or racemates and/or resolving a racemate into the optical isomers.

In starting compounds and intermediates which are converted to the compounds of the invention in a manner described herein, functional groups present, such as carboxy, amino (including ring NH) and hydroxy groups, are optionally protected by conventional protecting groups that are common in preparative organic chemistry. Protected carboxy, amino and hydroxy groups are those that can be converted under mild conditions into free carboxy, amino and hydroxy groups without the molecular framework being destroyed or other undesired side reactions taking place. The purpose of introducing protecting groups is to protect the functional groups from undesired reactions with reaction components and under the conditions used for carrying out a desired chemical transformation. The need and choice of protecting groups for a particular reaction is known to those skilled in the art and depends on the nature of the functional group to be protected (carboxy group, amino group, etc.), the structure and stability of the molecule of which the substituent is a part, and the reaction conditions. Well-known protecting groups that meet these conditions and their introduction and removal are described, for example, in J.F.W. McOmie, "Protective Groups in Organic Chemistry", Plenum Press, London, New York, 1973; T.W. Greene, "Protective Groups in Organic Synthesis", Wiley, New York, 1984.
Relating to the above processes, a reactive functional derivative of the radicals R, and R₂ represents said radicals substituted by a leaving group, preferably by lower alkyl-or aryl-sulfonyloxy, e.g. mesyloxy or toluenesulfonyloxy, or by halogen, e.g. fluoro, chloro, bromo or iodo. Similarly, a reactive esterified derivative of an alcohol, e.g. of. a compound of formula Vlll, represents said alcohol esterified in the form of a leaving group, e.g. lower alkyl-or aryl-sulfonyloxy, such as mesyloxy or toluenesulfonyloxy, or halogen, such as chloro, bromo or iodo.
Protecting groups for the imidazolyl nitrogen are preferably tri-lower alkylsilyl, e.g. trimethylsilyl, lower alkanoyl, e.g. acetyl, di-lower alkylcarbamoyl such as dimethylcarbamoyl, or triarylmethyl, e.g. triphenylmethyl.
The condensation according to process (a) is carried out according to N-alkylation procedures well- known in the art, either as such or in the presence of a base such as triethylamine or pyridine in an inert solvent, e.g. dichloromethane, at room temperature or near the boiling point of the solvent used.
A N-protected derivative of formula VII is particularly used, when a compound of formula I wherein W is 1-imidazolyl or lower-alkyl-substituted 1-imidazolyl is prepared. In the case of protected imidazolyl, alkylation occurs on the second unprotected nitrogen to first form a quaternary compound which is advantageously simultaneously deprotected in situ prior to the isolation of the product. The imidazole and triazole starting materials of formula VII are either known or are prepared according to methods known in the art.
The nitrile substituted starting materials representing reactive esterified derivatives of the carbinols of formula VIII are also either known or are prepared e.g. as illustrated below and in the examples herein. For example, the halo substituted starting materials can be advantageously prepared using the following illustrative sequence of reactions (tBu = tert-butyl) using appropriate reaction conditions known in the art and illustrated in the examples.
The starting materials of formula XIV represent appropriate aldehydes or ketones in which R, and R₂ correspond to relevant definitions in formula I.
For compounds of formula I wherein R, represents hydrogen and R₂ represents cyanophenyl, the intermediate corresponding to formula XV can be advantageously prepared by reacting the lithium organometallic reagent of formula XIII with ethyl formate (instead of a compound of formula XIV) in the above sequence of reactions.
It should also be noted that in the above intermediate XIII, the CONH-tBu substituent may be replaced by cyano or any other grouping suitable for the condensation and known in the art to be convertible into cyano. Such groupings are included under process (d) (R_s in formula XII).
The dehalogenation under process (b) for the preparation of the compounds of formula I wherein W represents pyridyl optionally substituted by lower alkyl can be achieved advantageously with zinc in acetic acid. Other suitable reagents include tributyl tin hydride or aluminium amalgam.
The starting halides of formula IX can be prepared from an alcohol with a halogenating agent, e.g. thionyl chloride as described under process (a). The alcohol can in turn be prepared by condensation of a compound of formula XIII or the like with an appropriate aldehyde or ketone of the formula XVII
W"-
-R, (or -R₂) (XVII)
in which R, and R2 correspond to relevant definitions for R, and R₂ in formula I and W" represents 3-pyridyl.
The condensation according to process (c) is carried out according to procedures generally known in the art for displacement e.g. of a halo, lower alkyl-or aryl-sulfonyloxy leaving group, e.g. by first forming a carbanion in the presence of a strong base such as lithium diisopropylamide, an alkali metal hydride, an alkali metal alkoxide such as potassium t-butoxide, or a strongly basic tertiary amine such as 1,5-diazabicyclo[4.3.0]non-5-ene (DBN), preferably in an inert atomosphere, for example under a nitrogen atmosphere, and in a polar solvent such as dimethylformamide.
For compounds of formula I wherein R, and/or R₂ represents p-cyanophenyl a suitable reactive derivative is p-fluorobenzonitrile. For compounds wherein R, or R2 represents (lower alkyl, aryl or aryl-lower alkyl)-thio, suitable reactive derivatives are the disulfides corresponding thereto, such as diphenyl disulfide or dimethyl disulfide.
Process (d) is carried out according to known methods for the introduction of a nitrile group.
A group or radical R_s in a compound formula XII which can be converted into the CN group, is, for example, hydrogen, esterified hydroxy, for example halo, especially chloro, bromo, or iodo, or a sulfonyloxy group, for example p-toluenesulfonyloxy, benzenesulfonyloxy or mesyloxy, sulfo, amino, carboxy, carboxy in the form of a functional derivative, for example carbamoyl, lower alkylcarbamoyl, for example t-butylcarbamoyl, or haloformyl, for example chloro-or bromoformyl, formyl, a formyl group in the form of a functional derivative, for example hydroxyiminomethyl, or a halomagnesium group, for example iodo-, bromo-or chloromagnesium.
Compounds of the formula I (or II-VI) can be obtained, for example, by carrying out the following conversions:

The conversion of a compound of the formula Xll wherein R_s is hydrogen, to the corresponding nitrile of the formula I is performed e.g. according to the known method of C. Friedel, F.M. Crafts and P. Karrer by reacting with cyanogen chloride (CICN) or cyanogen bromide or according to the method of J. Houben and W. Fisher, by reacting with e.g. trichloroacetonitrile. Advantageously, the standard catalyst aluminium chloride is used in these reactions and hydrogen chloride or hyrogen bromide is released which can be removed from the reaction mixture after addition of a base, preferably an amine, for example triethylamine or pyridine.

The conversion of a compound of the formula XII wherein R_s is halo, for example, chloro, bromo or iodo, to a corresponding nitrile of the formula I is performed by using e.g. a cyanide salt, especially sodium or potassium cyanide or, preferably, copper(l) cyanide. Preferred solvents for this reaction are pyridine, quinoline, dimethylformamide, 1-methyl-2-pyrrolidinone and hexamethylphosphoric triamide. High temperatures, especially reflux temperatures of the reaction mixture are preferred.
The conversion of a compound of the formula XII wherein R_s is a sulfonyloxy group, for example p-toluenesulfonyloxy, benzenesulfonyloxy or mesyloxy, to a nitrile of the formula I is performed e.g. by reaction with an alkali metal cyanide, preferably sodium or potassium cyanide. High temperatures, expecially the reflux temperature of the reaction mixture, are preferred.
The conversion of a compound of the formula XII wherein R_s is amino, to a nitrile of the formula I proceeds over several steps. First, a diazonium salt is formed e.g. by reaction of the amino compound with an alkali metal nitrite preferably potassium nitrite. The diazonium salt can be reacted using the well-known Sandmeyer reaction in situ e.g. with cuprous cyanide or a cyanide complex preferably potassium cuproammonium cyanide, or with catalytic amounts of freshly precipitated copper powder in the presence of an alkali metal cyanide, for example sodium or potassium cyanide.
The conversion of a compound of formula XII wherein R_s is carboxy to a nitrile of formula I can be carried out e.g. by reaction with chlorosulfonylisocyanate in e.g. dimethylformamide according to the method of R. Graf, Angew. Chem. 80 , 183 (1968).
The conversion of a compound of the formula XII wherein R_s is a carboxy group in the form of a functional derivative, for example carbamoyl, lower alkylcarbamoyl, advantageously t-butylcarbamoyl, to a nitrile of the formula I can be carried out e.g. with a strong dehydrating agent, such as phosphorous pentoxide, phosphoryl chloride, thionyl chloride, phosgene or oxalyl chloride. The dehydration can be preferably carried out in the presence of a suitable base. A suitable base is, for example, an amine, for example a tertiary amine, for example tri-lower alkylamine, for example trimethylamine, triethylamine or ethyl diisopropylamine, or N,N-di-lower alkylaniline, for example N,N-dimethylaniline, or a cyclic tertiary amine, for example a N-lower alkylated morpholine, for example N-methylmorpholine, or is, for example, a base of the pyridine type, for example pyridine or quinoline.
The conversion of a compound of formula XII wherein R_s is formyl to a nitrile of formula I is carried out e.g. by converting the formyl group to a reactive functional derivative, for example a hydroxyiminomethyl group, and converting this group to cyano by a dehydrating agent. A suitable dehydrating agent is one of the inorganic dehydrating agents mentioned above, for example phosphorous pentachloride, or, preferably, the anhydride of an organic acid, for example the anhydride of a lower alkane carboxylic acid, for example acetic acid anhydride. The conversion of the formyl group to hydroxyiminomethyl is carried out by reaction a compound of formula XII wherein R_s is formyl, e.g. with an acid addition salt of hydroxylamine, preferably the hydrochloride.
A compound of the formula XII wherein R_s is formyl can also be converted directly to a corresponding nitrile of the formula I e.g. by reaction with O,N-bis(trifluoroacetyl)-hydroxylamine in the presence of a base, for example pyridine, according to the method of D. T. Mowry, Chem. Rev. 42, 251 (1948).
The conversion of a compound of the formula XII wherein R_s is a halomagnesium group, for example, iodo-, brom-, or chloromagnesium, to a corresponding nitrile of the formula I is performed e.g. by reacting the magnesium halide with cyanogen halide or dicyanogen. The "Grignard" reagent, wherein R_s is a halomagnesium group, is prepared in a conventional manner, for example by reacting a compound of the formula XII wherein R_s is halo, for example chloro, bromo or iodo, with magnesium, e.g. in dry ether.
The compounds of the invention obtained by the above-cited processes can be converted into other compounds of the invention of formula I according to methodology known in the art and as illustrated herein.
Compounds of formula I, substituted by e.g. an acyloxy group, such as lower alkanoyloxy or aroyloxy, may be converted to compounds of formula I substituted by hydroxy, by hydrolysis with e.g. aqueous acid such as hydrochloric acid, or with aqueous alkali, such as lithium or sodium hdyroxide.
Conversely, the conversion of compounds of formula I substituted by hydroxy to compounds of formula I substituted by acyloxy, such as alkanoyloxy or aroyloxy, may be carried out by condensation with a corresponding carboxylic acid, or a reactive functional derivative thereof, according to acylation - (esterification) procedures wellknown to the art.
The conversion of the compounds of formula I substituted by an etherified hydroxy group, e.g. lower alkoxy, to the compounds of formula I substituted by a hydroxy group is carried out by methods well-known in the art, e.g., with a mineral acid, such as hydriodic acid or, advantageously for compounds wherein lower alkoxy is methoxy, with e.g. boron tribromide in methylene chloride or with sodium or lithium diphenyl- phosphide in tetrahydrofuran.
The compounds of formula I wherein R, and R₂ represent hydrogen, i.e. the compounds of formula XI, may be converted to the compounds of formula I wherein R, and R₂ combined represent lower alkylidene, mono-or diaryl-lower alkylidene by reacting said compounds of formula XI with an appropriate aldehyde or ketone in the presence of a strong base, e.g. lithium diisopropylamide, and, if required, treating the resulting alcohols with a dehydrating agent, such as thionyl chloride.
Furthermore, the compounds of formula I wherein at least one of R, and R₂ represents hydrogen are converted to other compounds of formula I as described above under process c).
Unless stated otherwise, the above reactions are preferably carried out in an inert, preferably anhydrous, solvent or solvent mixture, for example in a carboxylic acid amide, for example a formamide, for example dimethylformamide, a halogenated hydrocarbon, for example methylene chloride or chloroform, a ketone, for example acetone, a cyclic ether, for example tetrahydrofuran, an ester, for example ethyl acetate, or a nitrile, for example acetonitrile, or in mixtures thereof, optionally at reduced or elevated temperature, for example in a temperature range from approximately -50°C to approximately +150°C, preferably from room temperature to the boiling temperature of the reaction mixture and optionally under inert gas atmosphere, for example nitrogen atmosphere, and preferably at atmospheric pressure.
The invention further includes any variant of the present processes, in which an intermediate product obtainable at any stage thereof is used as starting material and the remaining steps are carried out, or the process is discontinued at any stage thereof, or in which the starting materials are formed under the reaction conditions or in which the reaction components are used in the form of their salts or optically pure antipodes. Whenever desirable, the above processes are carried out after first suitably protecting any potentially interfering reactive functional groups, as illustrated above and in the examples herein.
Advantageously, those starting materials should be used in said reactions, that lead to the formation of those compounds indicated above as being preferred.
The invention also relates to novel starting materials and processes for their manufacture.
Depending on the choice of starting materials and methods, the new compounds may be in the form of one of the possible isomers or mixtures thereof, for example, as pure geometric isomers (cis or trans), as pure optical isomers (as antipodes), or as mixtures of optical isomers such as racemates, or as mixtures of geometric isomers.
In case geometric or diastereomeric mixtures of the above compounds of intermediates are obtained, these can be separated into the single racemic or optically active isomers by methods in themselves known, e.g. by fractional distillation, crystallization and/or chromatography.
The racemic products or basic intermediates can be resolved into the optical antipodes, for example, by separation of diastereomeric salts thereof, e.g., by the fractional crystallization of d-or I-(tartrate, dibenzoyltartrate, mandelate or camphorsulfonate) salts.
Any acidic intermediates or products can be resolved by separation of e.g. the d-and I-(alpha- methylbenzylamine, cinchonidine, cinchonine, quinine, ephedrine, dehydroabietylamine, brucine or strychnine)-salts of any compounds having an acidic salt-forming group.
Advantageously, the more active of the antipodes of the compounds of this invention is isolated.
Finally, the compounds of the invention are either obtained in the free form, or as a salt thereof. Any resulting base can be converted into a corresponding acid addition salt, preferably with the use of a pharmaceutically acceptable acid or anion exchange preparation, or resulting salt can be converted into the corresponding free bases, for example, with the use of a stronger base, such as a metal or ammonium hydroxide, or any basic salt, e.g., an alkali metal hydroxide or carbonate, or a cation exchange preparation. These or other salts, for example, the picrates, can also be used for purification of the bases obtained; the bases are converted into salts. In view of the close relationship between the free compounds and the compounds in the form of their salts, whenever a compound is referred to in this context, a corresponding salt is also intended, provided such is possible or appropriate under the circumstances.
The compounds, including their salts, may also be obtained in the form of their hydrates, or include other solvents used for the crystallization.
The pharmaceutical compositions according to the invention are those suitable for enteral, such as oral or rectal, transdermal and parenteral administration to mammals, including man, comprising an effective amount of a pharmacologically active compound of formula I, or 11, III, IV, V or VI or a pharmacologically acceptable salt thereof, alone or in combination with one or more pharmaceutically acceptable carriers.
The pharmacologically active compounds of the invention are useful in the manufacture of pharmaceutical compositions comprising an effective amount thereof in conjunction or admixture with excipients or carriers suitable for either enteral or parenteral application. Preferred are tablets and gelatin capsules comprising the active ingredient together with a) diluents, e.g. lactose, dextrose, sucrose, mannitol, sorbitol, cellulose and/or glycine; b) lubricants, e.g. silica, talcum, stearic acid, its magnesium or calcium salts and/or polyethyleneglycol; for tablets also c) binders, e.g. magnesium aluminium silicate, starch paste, gelatin, tragacanth, methylcellulose, sodium carboxymethylcellulose and/or polyvinylpyrrolidone; if desired, d) disintegrants, e.g. starches, agar, alginic acid or its sodium salt, or effervescent mixtures; and/or e) e.g. absorbents, colorants, flavors and sweeteners. Injectable compositions are preferably aqueous isotonic solutions or suspensions, and suppositories are advantageously prepared from fatty emulsions or suspensions. Said compositions may be sterilized and/or contain adjuvants, such as preserving, stabilizing, wetting or emulsifying agents, solution promoters, salts for regulating the osmotic pressure and/or buffers. In addition, the compositions may also contain other therapeutically valuable substances. Said compositions are prepared according to conventional mixing, granulating or coating methods, respectively, and contain preferably about 1 to 50% of the active ingredient.
The dosage of active compound administered is dependent on the species of warm-blooded animal - (mammal), the body weight, age and individual condition, and on the form of administration. A unit dosage for a mammal of about 50 to 70 kg may contain between about 5 and 100 mg of the active ingredient.
Suitable formulations for transdermal application include an effective amount of a compound of formula I or II-VI with carrier. Advantageous carriers include absorbable pharmaceutically acceptable solvents to assist passage through the skin of the host. Characteristically, transdermal devices are in the form of a bandage comprising a backing member, a reservoir containing the compound, optionally with carriers, optionally a rate controlling barrier to deliver the compound to the skin of the host at a controlled and predetermined rate over a prolonged period of time, and means to secure the device to the skin.
The following examples are intended to illustrate the invention and are not to be construed as being limitations thereon. Temperatures are given in degrees Centigrade. If not mentioned otherwise, all evaporations are performed under reduced pressure, preferably between about 20 and 130 mbar. The structure of final products, intermediates and starting materials is confirmed by analytical methods, e.g. microanalysis and spectroscopic characteristics (e.g. MS, IR, NMR). The following abbreviations are used: HCI = hydrochloric acid, THF = tetrahydrofuran, DMF = dimethylformamide.
Example 1: a) A solution of aipha-bromo-4-totunitriie (86.6 g) in dichloromethane (1000 ml) is mixed with imidazole (68.0 g). The mixture is stirred at ambient temperature for 15 h and then diluted with water (1000 ml). Any undissolved solid is removed by filtration and the separated organic solution is then repeatedly washed with water (5 x 200 ml) to remove excess imidazole, and then dried (MgSO.). The crude product obtained upon evaporation of the solvent can be purified by trituration with cold diethyl ether (200 ml) to obtain 4-(1-imidazolylmethyl)-benzonitrile, m.p. 99-101 °; HCI salt, m.p. 142-144°.
Similarly prepared are:

b) 2-(1-imidazolylmethyl)-benzonitrile hydrochloride, m.p. 176-177°;
c) 4-(1-imidazolylmethyl)-1-naphthonitrile hydrochloride, m.p. 210-212° (dec.).

Example 2: a) A suspension of potassium tert-butoxide (61.6 g) in DMF (500 ml) is stirred and cooled to -10° (ice-salt bath), and a solution of 4-(1-imidazolylmethyl)-benzonitrile (45.6 g) in DMF (250 ml) is added so that the reaction temperature remains below 0°. The resulting solution is stirred at 0° for 0.5 h and then a solution of 4-fluorobenzonitrile (38.3 g) in DMF (100 ml) is added while keeping reaction temperature below 5°. After 0.75 h, the reaction mixture is neutralized to pH 7 by addition of sufficient 3N HCI and the bulk of the solvents are then removed under reduced pressure. The residue is diluted with water (500 ml) and the crude product is extracted into ethyl acetate (3 x 200 ml). The combined extracts are then extracted with 3N HCI (3 x 150 ml) and, after washing the latter acid extracts with ethyl acetate (100 ml), the solution is made basic (pH.8) with 6N ammonium hydroxide and the product is again extracted into ethyl acetate (3 x 150 ml). The combined extracts are dried (MgS04), decolorized by treatment with charcoal, and then evaporated to give crude 4-[alpha-(4-cyanophenyl)-1-imidazolylmethyl]-benzonitrile as an oil. This material is dissolved in isopropanol (250 ml) and the warm solution is stirred with succinic acid (14.4 g). Upon dilution with diethyl ether (100 ml) and stirring at ambient temperature, the hemisuccinate salt separates. The salt is filtered off, washed with a little cold isopropanol and then air-dried to afford 4-[alpha-(4-cyanophenyl)-l-imidazolylmethyl]-benzonitrile hemisuccinate, m.p. 149-150⁰. The hemifumarate salt has m.p. 157-158°.
Similarly prepared are:

b) 4-[alpha-(2-cyanophenyl)-l-imidazolylmethyl]-benzonitrile, IR(CN) 2240 cm-', M/e 384; HCI salt - (hygroscopic), m.p. 90° (dec.);
c) 4-[alpha-(4-trifluoromethylphenyl)-1-imidazolyimethyl]-benzonitrile, IR(CN) 2232 cm-', M/e 327; HCI salt - (hygroscopic), m.p. 100° (dec.).

Example 3: A solution of 4-(alpha-chloro-4'-cyanobenzyl)-benzonitrile (20.2 g) and imidazole (16.3 g) in DMF (130 ml) is stirred and heated at 160° for 2 h. The reaction is cooled, diluted with water (800 ml) and extracted into ethyl acetate (3 x 150 ml). The remainder of the work-up is carried out in the manner described in Example 2 to yield 4-[alpha-(4-cyanophenyl)-1-imidazolylmethyl]-benzonitrile hemisuccinate, m.p. 148-150°.
The starting material, 4-(alpha-chloro-4'-cyanobenzyl)-benzonitrile is prepared as follows:

A solution of N-tert-butyl-4-bromobenzamide (37.2 g) in anhydrous THF (1000 ml) is stirred under an atmosphere of N₂ and cooled to -60°. A solution of n-butyl lithium (125 ml, 2.4 M in hexane, 0.300 mole) is then added during 40 min and the resulting suspension is stirred for a further 40 min at -60°. A solution of ethyl formate (5.3 g) in anhydrous THF (50 ml) is then added dropwise during 10 min and the reaction is allowed to proceed at -60° for 2 h. The reaction is then quenched by the addition of saturated aqueous ammonium chloride (200 ml) and after allowing the mixture to reach room temperature, diethyl ether (300 ml) is added and the layers are separated. The ethereal solution is washed with water (2 x 100 ml) and brine (100 ml) and dried (MgS04). The solvent is evaporated and the residue is triturated with diethyl ether - (150 ml) to afford the bis-(4-N-tert-butylcarbamoylphenyi)methanol, m.p. 200-202°.

Bis-(4-N-tert-butylcarbamoylphenyl)-methanol (17.6 g) is suspended in thionyl chloride (140 ml) and the mixture is stirred at reflux for 6 h. The solvent is evaporated and the residue is taken up in toluene (100 ml) and the solvent is evaporated. The latter procedure is repeated once more to afford the 4-(alpha-chloro-4'-cyanobenzyl)-benzonitrile as an oil which is used directly; NMR(CH methine) 3.85 ppm.
Example 4: Imidazole (9.4 g) and 4-(alpha-chloro-4'-cyanobenzyl)-benzonitrile (11.6 g) are intimately mixed and heated together in an oil bath at 110-120° for 15 h. The reaction mixture is diluted with water - (200 ml) and extracted with ethyl acetate (3 x 75 ml). The remainder of the work-up is carried out as described in Example 2, yielding 4-[alpha-(4-cyanophenyl)-1-imidazolylmethyl)-benzonitrile. The crude product is treated with an equivalent amount of fumaric acid in warm isopropanol to yield 4-[alpha-(4-cyanophenyl)-1-imidazolylmethyl]-benzonitrile hemifumarate, m.p. 156-157⁰.
Example 5: The following compounds are prepared according to the methods described in previous examples 3 and 4 using the appropriate starting materials.

a) 2-[alpha-(4-bromophenyl)-1-imidazolylmethyl)-benzonitrile, M/e 337;
b) 4-[alpha-(4-chlorophenyl)-1-imidazolylmethyl]-benzonitrile; M/e 293; hydrochloride salt, m.p. 90° - (dec.);
c) 4-[alpha-(4-methoxyphenyl)-1-imidazolylmethyl]-benzonitrile, IR(CN) 2235 cm-', M/e 289; hydrochloride salt (hygroscopic), m.p. 90° (dec.);
d) 4-[alpha-(2-methoxyphenyl)-1-imidazolylmethyl]-benzonitrile, IR(CN) 2234 cm-', M/e 289; hydrochloride salt (hygroscopic), m.p. 95° (dec.);
e) 4-[alpha-(3-pyridyl)-1-imidazolylmethyl]-benzonitrile, IR(CN) 2237 cm-', M/e 260; dihydrochloride salt (hygroscopic), m.p. 150°;
f) 4-[alpha-(2-thienyl)-1-imidazolylmethyl]-benzonitrile, IR(CN) 2237 cm-'; M/e 265; hydrochloride salt, m.p.65° (dec.);
g) 4-[alpha-(3-thienyl)-1-imidazoly(methyl]-benzonitrile, IR(CN) 2240 cm^-1, M/e 265; hydrochloride salt, m.p. 70° (dec.);
h) 4-(alpha-phenyl-1-imidazolylmethyl)-benzonitrile; M/e 259; hydrochloride salt (hygroscopic), m.p. 90 (dec.);
i) 4-[alpha-(4-tolyl)-1-imidazolylmethyl]-benzonitrile; M/e 273; hydrochloride salt (hygroscopic), m.p. 90 (dec.);
j) 3-(alpha-phenyl-1-imidazolylmethyl)-benzonitrile; M/e 259; hydrochloride salt (hygroscopic), m.p. 80 (dec.);

The starting precursor for compound b is prepared as follows: A solution of n-butyl lithium (20 ml of 2.4 M reagent, 0.048 mole) in hexane is added dropwise under an atmosphere of N₂ to a solution of N-tert-butyl-4-bromobenzamide (6.1 g, 0.024 mole) in THF (100 ml) which is maintained at -60° and then a solution of 4-chlorobenzaldehyde (5.1 g, 0.036 mole) in THF (50 ml) is added dropwise. The reaction mixture is stirred for 2 h at -60° and then quenched by the addition of saturated aqueous ammonium chloride (30 ml) and ether (100 ml). The ethereal layer is separated, washed repeatedly (3 x 30 ml) with aqueous sodium bisulfite and finally with brine and dried (MgSO₄). Solvent evaporation affords (4-chlorophenyl)-(4'-N-tert-butylcarbamoylphenyl)-methanol as an oil, NMR(CH methine) 4.30 ppm, which can be used without further purification.
The following carbinols are prepared in a similar manner using an appropriate starting material:

phenyl-(4'-N-tert-butylcarbamoylphenyl)-methanol, NMR(CH methine) 4.27 ppm;
(4-methoxyphenyl)-(4'-N-tert-butylcarbamoylphenyl)-methanol, NMR(CH methine) 4.23 ppm;
(2-methoxyphenylr(4'-N-tert-butylcarbamoylphenyl)-methanol, NMR(CH methine) 4.00 ppm;
(4-methylphenyl)-(4'-N-tert-butylcarbamoylphenyl)-methanol, NMR(CH methine) 4.23 ppm;
(3-pyridyl)-(4'-N-tert-butylcarbamoylphenyl)-methanol, NMR(CH methine) 4.20 ppm;
(2-thienyl)-(4'-N-tert-butylcarbamoylphenyl)-methanol, NMR(CH methine) 3.98 ppm;
(3-thienyl)-(4'-N-tert-butylcarbamoylphenyl)-methanol, NMR(CH methine) 4.05 ppm;
3-(alpha-hydroxybenzyl)-benzonitrite, NMR(CH methine) 4.20 ppm.

The appropriate starting cyanophenyl substituted chlorides corresponding to the above carbinols are prepared by treatment with thionyl chloride as previously described in Example 3.
Example 6: A solution of 4-[alpha-(4-cyanophenyl)-1-imidazolylmethyl]-benzonitrile (5.3 g) in DMF (20 ml) is added dropwise to a cooled (ice-bath) stirred suspension of potassium tert-butoxide (2.5 g) in DMF - (20 ml). This mixture is stirred for 30 min at 0-5° and then a solution of methyl iodide (3,5 g) in DMF (10 ml) is added during 10 min. After stirring at 0-5° for a further 15 min, the reaction mixture is diluted with water (200 ml) and extracted with ethyl acetate (3 x 60 ml). The organic solution is washed with water (50 ml) and then extracted with 3N HCI (3 x 30 ml). The extracts are made basic (pH 8) with aqueous sodium hydroxide and the product is again extracted into ethyl acetate (2 x 50 ml). The extracts are dried (MgSO₄) and evaporated to give a solid which is recrystallized from isopropanol to give 4-[alpha-(4-cyanophenyl)-alpha-methyl-1-imidazolylmethyl]-benzonitrile, m.p. 184-186°.
Example 7: a) A solution of boron tribromide (11.7 g) in dichloromethane (50 ml) is added dropwise during 30 min to a cooled (ice-bath) stirred solution of 4-[alpha-(4-methoxyphenyl-1-imidazolylmethyl]-benzonitrile (3.2 g) in dichloromethane (50 ml). The reaction is allowed to proceed at ambient temperature for 15 h and then the mixture is poured onto ice and water (100 ml). The pH is adjusted to 7 by the addition of solid sodium bicarbonate and the layers are separated. The organic solution is washed with water, dried (MgSO₄) and evaporated. The residual crude product is triturated with diethyl ether to give 4-[alpha-(4-hydroxyphenyl)-1-imidazolylmethyl]-benzonitrile, m.p. 196-198°.

b) 4-[alpha-(2-hydroxyphenyl)-1-imidazolylmethyl]-benzonitrile, m.p. 230-235° (dec.), is similarly prepared.
c) 4-[alpha-(4-hydroxybenzyl)-1-imidazolylmethyl]-benzonitrile, m.p. 238-240°, is also similarly prepared.

Example 8: A solution containing 2-[alpha-(4-bromophenyl)-1-imidazolylmethyl]-benzonitrile (2.1 g) and hydrazine hydrate (10 ml) in 95% ethanol (60 ml) is mixed with 10% Pd-C catalyst (0.5 g) and the mixture is stirred at reflux for 2.5 h. The catalyst is filtered off and the solvent evaporated to give an oil which is dissolved in 3N HCI (20 ml). The acid solution is extracted with ethyl acetate (10 ml), neutralized to pH 7 with aqueous sodium hydroxide and extracted with ethyl acetate (3 x 10 ml). The extracts are dried - (MgSO₄) and evaporated to give the crude product which is further purified by flash column chromatography on silica gel. Elution with ethyl acetate affords 2-[alpha-pheny(-1-imidazolylmethyl]-benzonitrile; IR(CN): 2240 cm-'; M/e 259; hydrochloride salt. melting with dec.
Example 9: A solution containing alpha-bromo-4-tolunitrile (19.6 g) and 1,2,4-triazole (30.5 g) in a mixture of chlorform (250 ml) and acetonitrile (50 ml) is stirred at reflux for 15 h. The solution is cooled and washed with 3% aqueous sodium bicarbonate (200 ml) and the organic solution is then dried (MgSO.) and evaporated. The residue is chromatographed on silica gel (300 g). Elution with chloroform/isopropanol - (10:1) affords 4-[1-(1,2,4-triazolyl)methyl]-benzonitrile, which forms a hydrochloride salt, m.p. 200-205°, when its solution in ethyl acetate is treated with ethereal HCI.
Further elution of the silica gel column with chloroform/isopropanol (3:2) affords 4-[i-(1,3,4-triazolyl)-methyl]-benzonitrile which forms a hydrochloride salt, m.p. 236-238°.
Example 10: A solution containing alpha-bromo-4-tolunitrile (11.0 g), 1-(dimethylcarbamoyl)-4-methylimidazole (8.6 g) and sodium iodide (8.4 g) in acetonitrile (75 ml) is heated and stirred at reflux for 15 h. The mixture is cooled to 0° (ice-bath) and ammonia gas is bubbled through the solution for 15 min. The volatiles are then evaporated and the residue is partitioned between water (150 ml) and ethyl acetate (150 ml). The organic solution is washed with water (2 x 50 ml) and is then extracted with 3N HCI. The combined acidic extracts are made basic (pH 9) with 6N sodium hydroxide and the product is extracted into ethyl acetate (3 x 60 ml). After drying (MgSO,), solvent evaporation affords crude 4-[1-(5-methylimidazolyl)-methyl]-benzonitrile which forms a hydrochloride salt, m.p. 203-205°, when its solution in acetone is treated with ethereal HCI.
The starting material is prepared in the following manner: A solution containing 4-methylimidazole (16.4 g), N,N-dimethylcarbamoyl chloride (30 g) and triethylamine (30 g) in acetonitrile (125 ml) is stirred at reflux for 20 h. Upon cooling, the reaction is diluted with diethyl ether (1000 ml) and then filtered. The filtrate is concentrated and the residue is distilled under reduced pressure. 1-(Dimethylcarbamoyl)-4-methylimidazole is obtained as a colorless liquid, b.p. 104-106° at 0.47 mbar.
Example 11: a) A solution of n-butyl lithium (25 ml of 2.1 M reagent in hexane, 0.0525 mole) is added dropwise in an N2 atmosphere to a solution of diisopropylamine (5.6 g) in THF (100 ml) which is maintained at -20°. This cold solution is then added dropwise to a solution of 4-(1-imidazolylmethyl)-benzonitrile (9.15 g) in THF (250 ml) which is maintained at -50° during addition and for 30 min subsequently. The reaction mixture is then cooled to -70° for 30 min and then without external cooling for 10 h. The reaction is quenched by addition of water (300 ml) and extracted with diethyl ether (3 x 100 ml). The combined ether extracts are extracted with 3N HCI (3 x 60 ml) and the acid extracts are made basic (pH 9) with 6N sodium hydroxide. The crude product is extracted into ether (3 x 60 ml), and after drying (MgS04) and solvent evaporation, 4-[1-(1-imidazolyl)ethyl]-benzonitrile is obtained. The crude material is dissolved in acetone and treated with ethereal HCI to afford the hydrochloride salt, m.p. 184-186°.
Similarly prepared are:

b) 4-[2-(1-imidazolyl)-2-propyl]-benzonitrile hydrochloride, m.p. 219-2210;
c) 4-(alpha-n-butyl-1-imidazolylmethyl)-benzonitrile oxalate, m.p. 73-75°;
d) 4-(alpha-isopropyl-1-imidazolylmethyl)-benzonitrile, m.p. 94-95°;
e) 4-(alpha-benzyl-1-imidazolylmethyl)-benzonitrile hydrochloride, m.p. 221-223°;
f) 4-[alpha-(4-cyanobenzyl)-1-imidazolylmethyl]-benzonitrile. m.p. 199-201°;

Example 12: The lithium salt of 10.0 g of 4-(1-imidazolylmethyl)-benzonitrile is prepared in THF (250 ml) in the manner described in Example 11. This solution is cooled to -60° and solid paraformaldehyde - (10.0 g, previously dried for 15 h in vacuo at 60°) is added, all at once. The reaction mixture is stirred at - 60° for 1 h and then without cooling for a further 15 h. The reaction is then quenched with water (200 ml) and worked up in the manner described in Example 11 to afford a mixture of 4-(alpha-hydroxymethyl-1-imidazolylmethyl)-benzonitrile and 4-(alpha-methylene-1-imidazolylmethyl)-benzonitrile which is chromatographed on silica gel (250 g). Elution with a mixture of methylene chloride and isopropanol (19:1 ) affords 4-(alpha-methylene-1-imidazolylmethyl)-benzonitrile. This compound forms a hydrochloride salt, m.p. 195-197°, when its solution in acetone is treated with ethereal HCI.
Example 13: a) Racemic 4-[1-(1-imidazolyl)ethyl]-benzonitrile (3.5 g) is dissolved in warm acetone (50 ml) and added to a solution of 1-tartaric acid (1.2 g) in warm acetone (300 ml). The mixture is allowed to stand at room temperature overnight and the tartrate salt is collected. This material is recrystallized four times from minimal volumes of anhydrous ethanol and the resultant material is converted to the free base by dissolution in water, making basic (pH 9) with dilute sodium hydroxide and isolating (-)-4-[1-(1-imidazolyl)ethyl]-benzonitrile which has an optical rotation [α]_D ²⁵ = -4.94°.
b) (+)-4-[1-(1-imidazolyl)ethyl]-benzonitrile is obtained in a similar manner using d-tartaric acid and has an optical rotation [α]_D ²⁵ = +4.89_°.
Each enantiomer forms a hydrochloride salt, m.p. 190-191°. when a solution in acetone is treated with ethereal HCI.
Example 14: A solution of potassium tert-butoxide (1.10 g) in THF (50 ml) is added dropwise to a solution of 4-[1-(1-imidazolyl)-4-chlorobutyl]-benzonitrile (2.50 g) in THF at 0° (ice-bath). The reaction is allowed to proceed at 0° for 30 min and is then allowed to warm to room temperature during 3 h. The reaction is then quenched with water (100 ml) and the mixture is subsequently extracted with ethyl acetate - (100 ml). The organic extract is extracted with 3N HCl (3 x 30 ml) and the combined acid extracts are made basic with 6N sodium hydroxide. The crude product is extracted into ethyl acetate (3 x 30 ml) and the combined extracts are dried (MgSO₄) and evaporated to afford 1-(4-cyanophenyl)-1-(1-imidazolyl)-cyclopentane as an oil. The compound is dissolved in acetone and treated with ethereal HCl to afford the hydrochloride salt, m.p. 217-219°.
The starting material, 4-[1-(1-imidazolyl)-4-chlorobutyl]-benzonitrile, is prepared as follows:

The lithium salt of 4-[1-imidazolylmethyl]-benzonitrile (3.7 g) is prepared at -50° in THF (100 ml) as described in Example 11, and the cold solution is then added dropwise to a solution of 1-chloro-4-iodobutane (8.7 g) in THF (60 ml) at -60°. The reaction is maintained at -60° for 2 h and is then quenched by addition of water (150 ml). The product is extracted as described in Example 11 and the chlorobutyl intermediate is obtained as an oil. The methine-CH (triplet) is observed at 4.77 ppm in the NMR spectrum. The material is used without further purification.

Example 15: A solution of potassium tert-butoxide (4.5 g) in THF (125 ml) is added dropwise during 1 h to a solution of 4-[1-imidazolylmethyl]-benzonitrile (3.66 g) and α,α'-dichloro-o-xylene (3.50 g) in THF (100 ml) which is maintained at 0° (ice-bath). The reaction mixture is subsequently stirred for a further 1 h without external cooling and is then quenched with water (200 ml) and extracted with ethyl acetate (150 ml). The organic extracts are then extracted with 3N HCI (3 x 80 ml) and the acidic extracts are made basic with 6N sodium hydroxide and the crude product is extracted into ethyl acetate (3 x 50 ml). The material obtained after drying (MgSO.) and solvent evaporation is chromatographed on silica gel (100 g). Elution with ethyl acetate affords the crystalline 2-(4-cyanophenyl)-2-(1-imidazolyl)-indane which is recrystallized from isopropanol, m.p. 150-152°.
Example 16: a) The lithium salt of 4-[1-imidazolylmethyl]-benzonitrile (3.7 g) is prepared at -50° in THF (100 ml) in the manner described in Example 11. This cold solution is then added dropwise to a solution of diphenyl disulfide (6.5 g) in THF (100 ml) at -50°. The reaction mixture is stirred for 2 h, then quenched by addition of water (150 ml) and worked up as described in Example 11 to afford 4-[alpha-phenylthio-1-imidazolylmethyl]-benzonitrile as an oil. The compound forms a hydrochloride salt, m.p. 159-162°, when its solution in ether is treated with ethereal HCI.

b) 4-[alpha-Methylthio-1-imidazolylmethyl]-benzonitrile hydrochloride, m.p. 137-140°, is similarly prepared.

Example 17: 2,2-Bis-(4-methoxyphenyl)-2-hydroxy-1-(1-imidazolyl)-1-(4-cyanophenyl)-ethane (10.2 g) is dissolved in thionyl chloride (25 ml) and the solution is stirred at room temperature for 36 h. The solvent is evaporated and the residue is chromatographed on silic gel (250 g). Elution with ethyl acetate affords the crystalline 2,2-bis-(4-methoxyphenyl)-1-(1-imidazolyl)-1-(4-cyanophenyl)-ethylene. The compound has m.p. 174-176° after recrystallization from isopropanol.
The starting material is prepared as follows:

The lithium salt of 4-(1-imidazolylmethyl)-benzonitrile (5.5 g) is prepared in THF (200 ml) in the manner described in Example 11. This cold solution is added dropwise to a solution of 4,4'-dimethoxybenzophenone (7.5 g) in THF (100 ml) at -60°. The reaction is allowed to proceed for 4 h at -60° and is then quenched by dropwise addition of acetic acid (0.5 ml) and then water (200 ml). After warming to room temperature, the mixture is diluted with ether (200 ml). The separated organic phase is washed with water (3 x 50 ml), dried over MgSO₄ and, after evaporating the solvents, the residue is chromatographed on silica gel (200 g). Elution with ethyl acetate affords 2,2-bis-(4-methoxyphenyl)-2-hydroxy-1-(1-imidazolyl)-1-(4-cyanophenyl)-ethane as a foam [NMR (CH-methine) 4.15 ppm].

Example 18: Treatment of 2,2-bis-(4-methoxyphenyl)-1-(1-imidazolyl)-1-(4-cyanophenyl)-ethylene with boron tribromide using procedure analogous to that described in Example 7 yields 2,2-bis-(4-hydroxyphenyl)-1-(1-imidazolyl)-1-(4-cyanophenyl)-ethylene hydrobromide, m.p. 178° (dec.).
Example 19: a) Zinc dust (23 g) is added in small portions over 15 min to a solution of 4-(alpha-chloro-3-pyridytmethyl)-benzonitrile hydrochloride (13.25 g) in a mixture of acetic acid (110 ml) and water (5 ml). The reaction mixture is stirred at room temperature for 3 h and is then filtered through a pad of Celite. The filtrate is concentrated and the residue is taken up in ether (250 ml) and washed with 3N sodium hydroxide (3 x 100 ml) and brine. After drying the ethereal solution (anhydrous Na₂SO₄), solvent evaporation affords crude 4-(3-pyridylmethyl)-benzonitrile. The compound forms a hydrochloride salt, m.p. 155-157°, when its solution in ethyl acetate is treated with ethereal HCI.
The starting material is prepared from (3-pyridyl)-(4'-N-tert-butylcarbamoylphenyl)-methanol by treatment with thionyl chloride as described in Example 3.
Similarly prepared are:

b) 4-[alpha-(3-pyridyl)-3'-pyridylmethyl]-benzonitrile, m.p. 125-127°;
c) 4-[alpha-(4-pyridyl)-3'-pyridylmethyl]-benzonitrile oxalate, m.p. 172-174°.

Examole 20: a) 4-[l-(1,2,4-Triazolyl)methyl]-benzonitrile is reacted with potassium tert-butoxide and 4-fluorobenzonitrile according to procedure in Example 2 to yield a 4-[alpha-(4-cyanophenyl)-1-(1,2,4-triazolyl)methyl]-benzonitrile, m.p. 181-183°.
b) 4-[1-(1,3,4-Triazolyl)methyl]-benzonitrile is similarly reacted with 4-fluorobenzonitrile to yield 4-[alpha-(4-cyanophenyl)-1-(1,3,4-triazolyl)methyl]-benzonitrile, m.p. 239-243°.
Examole 21: 4-(3-Pyridylmethyl)-benzonitrile is reacted with potassium tert-butoxide and 4-fluorobenzonitrile according to the procedure in Example 2 to yield 4-[aipha-(4-cyanophenyl)-3-pyridylmethyl]-benzonitrile hydrochloride, m.p. 120-125° (dec.).
Example 22: To 48.0 I of acetone under nitrogen is added 4.326 kg of potassium carbonate, 0.26 kg of potassium iodide, 3.2 kg of imidazole and 4.745 kg of alpha-chloro-4-tolunitrile. The mixture is stirred at 45° under nitrogen for 26 h. The reaction mixture is cooled, filtered and the solvent is evaporated at reduced pressure. The residue is redissolved in 40 I of methylene chloride, washed with 40 I of water and twice with 10 I of water. The organic phase is dried over magnesium sulfate and evaporated to yield the crude product which is stirred with 6.4 I of ether for 2 h. The solid is filtered, washed with 9 I of ether and dried at 40° and 26.7 mbar for 17 h to yield 4-(1-imidazolylmethyl)-benzonitrile, the compound of Example 1.
Example 23: In portions of approximately 500 g, 4.44 kg of potassium tert-butoxide is added to 25 l of DMF, precooled to -10°, without allowing the solvent temperature to rise above -4°. The solution is recooled to -8° and a solution of 3.3 kg 4-(1-imidazolylmethyl)-benzonitrile in 12.5 I of DMF is added within 3.3 h. The rate of addition is adjusted to maintain the reaction temperature at -7 ± 2°.
The solution is stirred for 45 min while cooling to -11 and a solution of 2.18 kg of 4-fluorobenzonitrile in 5 I of DMF is added over 3.5 h. The reaction temperature is maintained at 3 ± 4°. After 1.25 h, the pH of the reaction is brought to 7 with 3.0 I of concentrated HCI, stirred an additional 20 min and allowed to stand overnight. The solvent is removed by distillation at 10.7 mbar over 7 h. The resulting oil is partitioned between 25 I of methylene chloride and 35 I of water. The layers are separated. The aqueous phase is extracted with 7 I of methylene chloride and the combined organic phases are washed with 10 I of H₂0 and twice with 1.1 I of 3N HCI. The combined acidic layers are washed with 7 I of methylene chloride and added to a mixture of 10 kg of ice and 20 I of methyllene chloride. The solution is stirred and brought to pH 11 with 2.8 I of concentrated sodium hydroxide solution. The aqueous layer is separated and extracted with 5 I of methylene chloride. The combined organic phases are washed with 10 I of water and dried over magnesium sulfate. Filtration and evaporation at 45° and 10.7 mbar yields 4-[alpha-(4-cyanophenyl)-1-imidazolylmethyl]-benzonitrile as an oil; IR (CH₂Cl₂) 2240 cm-'.
A solution of 9.23 kg of the above free base in 19.1 I of isopropanol is treated with 0.45 kg of decolorizing carbon and after 15 min is filtered into a stirred solution of 1.84 kg of succinic acid in 31.4 I of isopropanol at 50°. The solution is stirred for 14 h at 50° and allowed to cool to room temperature. The resulting crystalline solid is collected by filtration, washed with 8 I of isopropanol and 5 I of diethyl ether and dried at 90° and 26.7 mbar for 28 h to yield 4-[alpha-(4-cyanophenyl)-1-imidazolylmethyl]-benzonitrile hemisuccinate, m.p. 149-150^0. Recrystallization from isopropanol/ether gives product melting at 151-152^0.
Example 24: Preparation of 10,000 tablets each containing 5 mg of the active ingredient:

Formula:

All the powders are passed through a screen with openings of 0.6 mm. Then the drug substance, lactose, magnesium stearate and half of the starch are mixed in a suitable mixer. The other half of the starch is suspended in 65 mI of water and the suspension is added to the boiling solution of the polyethylene glycol in 260 ml of water. The paste formed is added to the powders, which are granulated, if necessary, with an additional amount of water. The granulate is dried overnight at 35°, broken on a screen with 1.2 mm openings and compressed into tablets, using concave uppers bisected.
Analogously tablets are prepared containing one of the other compounds disclosed and exemplified herein.
Example 25: Preparation of 1,000 capsules each containing 10 mg of the active ingredient:

Formula:

Procedure:

All the powders are passed through a screen with openings of 0.6 mm. Then the drug substance is placed in a suitable mixer and mixed first with the magnesium stearate, then with the lactose and starch until homogeneous. No. 2 hard gelatin capsules are filled with 300 mg of said mixture each, using a capsule filling machine.
Analogously capsules are prepared, containing one of the other compounds disclosed and exemplified herein.
Example 26: 10 mI of 2N sulfuric acid are added to a solution of 2.60 g (10 mmole) 4-[alpha-(3-pyridyl)-1-imidazolylmethyl]-benzonitrile, the compound of example 5e), in 100 ml of ethanol, while stirring and cooling the solution in an ice bath; immediately crystals precipitate. After filtration, washing with ethanol and drying under high vacuum, 4-[alpha-(3-pyridyl)-1-imidazolylmethyl]-benzonitrile sulfate, m.p. 238-240°, is obtained.

Claims

1. The use of the compounds of the formula I

wherein R and R_o independently represent hydrogen or lower alkyl; or R and R_a located on adjacent carbon atoms and together when combined with the benzene ring to which they are attached form a naphthalene or tetrahydro-naphthalene ring; R, and R₂ independently represent hydrogen, lower alkyl, (lower alkyl, aryl or aryl-lower alkyl)-thio, lower alkenyl, aryl, aryl-lower alkyl, C₃-C₆-cycloalkyl, or C₃-C₆-cycloalkyl-lower alkyl; or R, and R₂ combined represent lower alkylidene, mono-or di-aryl-lower alkylidene; R, and R₂ combined also represent C₄-C₆-straight chain alkylene, lower alkyl-substituted straight chain alkylene or ortho-phenylene bridged-C₂-C₄-straight chain alkylene, each forming with the carbon atom attached thereto a corresponding optionally substituted or benzo-fused 5-, 6-or 7-membered ring; W represents 1-imidazolyl, 1-(1,2,4 or 1,3,4)-triazolyl or 3-pyridyl; or W represents 1-imidazolyl, 1-(1,2,4 or 1,3,4)-triazolyl or 3-pyridyl substituted by lower alkyl; and pharmaceutically acceptable salts thereof; as aromatase inhibitors.

2. The use according to claim 1 of the compounds of formula I, wherein R and R_a represent independently hydrogen or lower alkyl; or R and R_a located on adjacent carbon atoms and together when combined with the benzene ring to which they are attached form a naphthalene or tetrahydro-naphthalene ring; R, represents hydrogen, lower alkyl, aryl, aryl-lower alkyl or lower alkenyl; R₂ represents hydrogen, lower alkyl, aryl, aryl-lower alkyl, (lower alkyl, aryl or aryl-lower alkyl)-thio or lower alkenyl; or R, and R₂ combined represent lower alkylidene or C₁-C₆alkylene; W has meaning given above; and aryl within the above definitions represents phenyl or phenyl substituted by one or two substituents selected from lower alkyl, lower alkoxy, hydroxy, acyloxy, nitro, amino, halogen, trifluoromethyl, cyano, carboxy, carboxy functionalized in form of a pharmaceutically acceptable ester or amide, lower alkanoyl, aroyl, lower alkylsulfonyl, sulfamoyl, N-lower-alkylsulfamoyl or N,N-di-lower alkylsulfamoyl; or aryl within the above definitions also represents a heterocyclic aromatic radical selected from thienyl, indolyl, pyridyl and furyl, or a said heterocyclic radical monosubstituted by lower alkyl, lower alkoxy, cyano or halogen; and pharmaceutically acceptable salts thereof.

3. Compounds of the formula I

wherein R and R_a independently represent hydrogen or lower alkyl; or R and R_o located on adjacent carbon atoms and together when combined with the benzene ring to which they are attached form a naphthalene or tetrahydro-naphthalene ring; R, represents hydrogen; R₂ represents hydrogen, lower alkyl, lower alkenyl, aryl, aryl-lower alkyl, C₃-C₆-cycloalkyl, or C₃-C₆cycloalkyl-lower alkyl; or R, and R₂ combined represent lower alkylidene, or mono-or di-aryl-lower alkylidene, R, and R₂ combined also represent C₄-C₆-straight chain alkylene, lower alkyl-substituted straight chain alkylene or ortho-phenylene bridged-C₂-C₄-straight chain alkylene, to form with the carbon atom attached thereto a corresponding optionally substituted or benzo-fused 5-, 6-or 7-membered ring; W represents 1-imidazolyl, 1-(1,2,4 or 1,3,4)-triazolyl or 3-pyridyl; or W repre sents 1-imidazolyl, 1-(1,2,4 or 1,3,4)-triazolyl or 3-pyridyl substituted by lower alkyl; and pharmaceutically acceptable salts thereof.

4. Compounds according to claim 3 of the formula I, wherein R and R_o represent hydrogen; or R and R_o located on adjacent carbon atoms and together when combined with the benzene ring to which they are attached form a naphthalene ring; R, represents hydrogen; R2 represents hydrogen, lower alkyl, aryl or aryl-lower alkyl; or R, and R₂ combined represent lower alkylidene or di-aryl-lower alkylidene; R, and R₂ combined also represent C₄-C₆-straight chain alkylene or ortho-phenylene bridged-C₂-C₄-straight chain alkylene, to form with the carbon atom attached thereto a corresponding optionally benzo-fused 5-, 6-or 7- membered ring; W represents 1-imidazolyl, 1-(1,2,4 or 1,3,4)-triazolyl, 3-pyridyl, or 1-imidazolyl substituted by lower alkyl; and aryl within the above definitions represents phenyl or phenyl substituted by lower alkyl, lower alkoxy, hydroxy, halogen, trifluoromethyl or cyano; thienyl or pyridyl; and pharmaceutically acceptable salts thereof.

5. Compounds according to claim 3 of the formula I, wherein R and R_o independently represent hydrogen or lower alkyl; or R and R_o located on adjacent carbon atoms and together when combined with the benzene ring to which they are attached form a naphthalene or tetrahydro-naphthalene ring; R, represents hydrogen; R₂ represents hydrogen, lower alkyl, lower alkenyl, aryl, or aryl-lower alkyl; or R, and R₂ combined represent lower alkylidene or C₄-C₆-alkylene; W represents 1-imidazolyl or 1-imidazolyl substituted by lower alkyl; and aryl within the above definitions represents phenyl or phenyl substituted by one or two substituents selected from lower alkyl, lower alkoxy, hydroxy, acyloxy, nitro, amino, halogen, trifluoromethyl, cyano, carboxy, carboxy functionalized in form of a pharmaceutically acceptable ester or amide, lower alkanoyl, aroyl, lower alkylsulfonyl, sulfamoyl, N-lower alkylsulfamoyl or N,N-di-lower alkylsulfamoyl; or aryl within the above definitions also represents a heterocyclic aromatic radical selected from thienyl, indolyl, pyridyl and furyl, or a said heterocyclic radical monosubstituted by lower alkyl, lower alkoxy, cyano or halogen; and pharmaceutically accpetable salts thereof.

6. Compounds according to claim 3 of the formula II

wherein R,' represents hydrogen; R; represents hydrogen, lower alkyl, phenyl, pyridyl, thienyl or benzyl; or R₂' represents phenyl or benzyl, each monosubstituted on the phenyl ring by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, aroyloxy, nitro, halogen, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; or R₁' and R₂' combined represent together lower alkylidene, benzylidene or diphenylmethylidene; or R,' and R₂' combined represent together C₄-C₆ straight chain alkylene; R₃ represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.

7. Compounds according to claim 6 of the formula II, wherein R,' represents hydrogen; R₂' represents hydrogen, lower alkyl, pyridyl, benzyl or phenyl; or R₂' represents benzyl or phenyl, each monosubstituted on phenyl by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, halogen, nitro, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; R₃ represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.

8. Compounds according to claim 6 of the formula II, wherein R,' represents hydrogen; R₂' represents hydrogen, lower alkyl, benzyl, phenyl, or 3-or 4-pyridyl; or R₂' represents phenyl or benzyl, each monosubstituted on phenyl by cyano, halogen, lower alkoxy, lower alkyl or trifluoromethyl; R₃ represents hydrogen or lower alkyl at the 4-or 5-position; and pharmaceutically acceptable salts thereof.

9. Compounds according to claim 3 of the formula III

wherein R₂' represents 3-pyridyl, p-cyanobenzyl or p-cyanophenyl; and pharmaceutically acceptable salts thereof.

10. Compounds of the formula IV

wherein R₁' represents hydrogen; R₂' represents hydrogen, lower alkyl, phenyl, lower alkylthio, phenyl-lower alkylthio, phenylthio, pyridyl, thienyl or benzyl; or R; represents phenyl, phenyl-lower alkylthio, phenylthio or benzyl, each monosubstituted on the phenyl ring by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, aroyloxy, nitro, halogen, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; or R,' and R; combined represent together lower alkylidene, benzylidene, diphenylmethylidene; or R,' and R₂' combined represent together C₄-C₆ straight chain alkylene; R₃ represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.

11. Compounds according to claims 3 and 10 of the formula IV, wherein R,' represents hydrogen; R₂' represents hydrogen, lower alkyl, pyridyl; or R₂' represents benzyl or phenyl, each unsubstituted or monosubstituted on phenyl by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, halogen, nitro, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; R₃ represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.

12. Compounds according to claim 11 of the formula IV, wherein R₁' represents hydrogen; R; represents hydrogen, lower alkyl, benzyl, phenyl, or 3-or 4-pyridyl; or R₂' represents phenyl or benzyl, each monosubstituted on phenyl by cyano, halogen, lower alkoxy, lower alkyl or trifluoromethyl; R₃ represents hydrogen or lower alkyl at the 4-or 5-position; and pharmaceutically acceptable salts thereof.

13. Compounds according to claim 11 of the formula IV, wherein R₁' and R₃ represent hydrogen; R₂' represents 3-pyridyl, p-cyanobenzyl or p-cyanophenyl; and pharmaceutically acceptable salts thereof.

14. Compounds according to claim 3 of the formula V

wherein R,' represents hydrogen; R; represents hydrogen, lower alkyl, phenyl, pyridyl, thienyl or benzyl; or R₂' represents phenyl or benzyl, each monosubstituted on the phenyl ring by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, aroyfoxy, nitro, halogen, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; or R,' and R₂' combined represent together lower alkylidene, benzylidene or diphenylmethylidene; or R,' and R₂' combined represent together C₄-C₆ straight chain alkylene; R₃' represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.

15. Compounds according to claim 14 of the formula V, wherein R,' represents hydrogen; R₂' represents hydrogen, lower alkyl, benzyl, phenyl, or 3-or 4-pyridyl; or R2' represents phenyl or benzyl, each monosubstituted on phenyl by cyano, halogen, lower alkoxy, lower alkyl or trifluoromethyl; R₃' represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.

16. Compounds according to claim 14 of the formula V, wherein R,' and R₃' represent hydrogen; R₂' represents 3-pyridyl, p-cyanobenzyl or p-cyanophenyl; and pharmaceutically acceptable salts thereof.

17. Compounds of the formula VI

wherein R,' represents hydrogen; R; represents hydrogen, lower alkyl, phenyl, lower alkylthio, phenyl-lower alkylthio, phenylthio, pyridyl, thienyl, benzyl; or R₂' represents phenyl, phenyl-lower alkylthio, phenylthio or benzyl, each monosubstituted on the phenyl ring by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, aroyloxy, nitro, halogen, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; or R,' and R₂' combined represent together lower alkylidene, benzylidene or diphenylmethylidene; or R,' and R₂' combined represent together C₄-C₆ straight chain alkylene; R₁ represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.

18. Compounds according to claims 3 and 17 of the formula VI, wherein R,' represents hydrogen; R₂' represents hydrogen, lower alkyl, pyridyl; or R₂' represents benzyl or phenyl each unsubstituted or monosubstituted on phenyl by cyano, lower alkyl, lower alkoxy, hydroxy, lower alkanoyloxy, halogen, nitro, trifluoromethyl, lower alkanoyl, aroyl, lower alkylsulfonyl, carbamoyl, N-mono-or N,N-di-lower alkylcarbamoyl, sulfamoyl, N-mono-or N,N-di-lower alkylsulfamoyl; R, represents hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof.

19. Compounds according to claim 18 of the formula VI, wherein R,' and R, represent hydrogen; R₂' represents hydrogen, lower alkyl, benzyl, phenyl, or 3-or 4-pyridyl; or R₂' represents phenyl or benzyl each substituted on phenyl by cyano, halogen, lower alkoxy, lower alkyl or trifluoromethyl; and pharmaceutically acceptable salts thereof.

20. Compounds according to claim 18 of the formula VI, wherein R,' and R, represent hydrogen; R₂' represents 3-or 4-pyridyl, p-cyano-benzyl or p-cyanophenyl; and pharmaceutically acceptable salts thereof.

21. A compound of claim 3 being 4-(alpha-isopropyl-1-imidazolylmethyl)-benzonitrile. a stereoisomer or a mixture of stereoisomers thereof, or a pharmaceutically acceptable salt thereof.

22. A compound of claim 3 being 4-[alpha-(3-pyridyl)-l-imidazolylmethyl]-benzonitrile, a stereoisomer or a mixture of stereoisomers thereof, or a pharmaceutically acceptable salt thereof.

23. A compound of claim 3 being 4-[alpha-(4-cyanophenyl)-1-imidazolylmethyl]-benzonitrile, or a pharmaceutically acceptable salt thereof.

24. A compound of claim 3 being 4-(alpha-benzyl-1-imidazolylmethyl)-benzonitrile, a stereoisomer or a mixture of stereoisomers thereof, or a pharmaceutically acceptable salt thereof.

25. A compound of claim 3 being 2-(4-cyanophenyl)-2-(1-imidazolyl)-indane, or a pharmaceutically acceptable salt thereof.

26. Pharmaceutical preparations containing a compound according to any one of claims 3-25.

27. A compound according to any one of claims 3-25 for use in a method for the therapeutic treatment of the animal or human body.

28. A compound according to any one of claims 3-25 for use as aromatase inhibitor.

29. The use of a compound according to any one of claims 3-25 for the manufacture of pharmaceutical preparations.

30. Process for the manufacture of the compounds of the formula I according to claim 3, or salts thereof, which comprises

a) for compounds of formula I wherein W represents 1-imidazolyl or 1-triazolyl each optionally substituted by lower alkyl, condensing a compound of the formula VII
W'-H (VII)
wherein W' represents 1-imidazolyl or 1-triazolyl each optionally substituted by lower alkyl, or an N-protected derivative thereof, with a reactive esterified derivative of a compound of the formula VIII,

wherein R, R₀, R₁ and R₂ have meaning as defined herein for formula I;

b) for compounds wherein W represents 3-pyridyl optionally substituted by lower alkyl, dehalogenating a compound of the formula IX

wherein W" represents 3-pyridyl optionally substituted by lower alkyl, X represents halogen, preferably chloro, R and R₀ have meaning as defined herein for compounds of formula I and R, has meaning as defined herein for formula I; and if required reacting the resulting product of formula X

with a reactive derivative of the radical R₂ using process c) below;

c) condensing under basic conditions a compound of the formula XI,

(being a compound of formula I wherein R, and R₂ represent hydrogen) wherein R, R₀ and W have meaning as defined herein for formula I, with a reactive functional derivative of a radical R₁ or R₂ (R₁ or R₂ not representing hydrogen), so as to obtain a compound of formula I wherein only one of R, and R₂ represents hydrogen; or similarly condensing a compound of formula I so obtained with a reactive functional derivative of a radical R, or R₂ (R, or R₂ not representing hydrogen) to obtain a compound of formula I wherein neither R, nor R₂ represents hydrogen; or condensing a compound of the formula Xl with a reactive bifunctional derivative of R, and R₂ combined representing C₄-C₆ straight alkylene, lower alkyl substituted C₄-C₆ straight chain alkylene or 1,2-phenylene-bridged-C₂-C₄ straight chain alkylene to obtain a corresponding compound of formula I;

d) converting R₅ to cyano in a compound of the formula XII,

wherein W, R, R₀, R, and R₂ have meaning as defined above and R_s represents a group or radical that can be converted to the cyano group;
and/or converting a compound of formula I into another compound of formula I; and/or converting a free compound into a salt, and/or converting a salt into a free compound or into another salt; and/or separating a mixture of isomers or racemates into the single isomers or racemates and/or resolving a racemate into the optical isomers.

31. A process according to claim 30 for the manufacture of a compound of the formula I wherein R, represents hydrogen; R₂ represents 4-cyanophenyl; W, R and R₀ have meaning as defined in said claim; which comprises condensing under basic conditions a compound of the formula XI

with p-fluorobenzonitrile.

32. A process according to claim 31 for the manufacture of 4-[alpha-(4-cyanophenyl)-1-imidazolylmethyl]-benzonitrile.